NDC 71610-774 – Bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet, Film Coated · Oral
Product NDC71610-774
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076143
- Marketed since
- January 17, 2006
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 75 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71610-774-53 | 60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53) | Jan 22, 2024 |
| 71610-774-70 | 120 TABLET, FILM COATED in 1 BOTTLE (71610-774-70) | Jan 25, 2024 |
| 71610-774-80 | 180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80) | Jan 25, 2024 |
| 71610-774-94 | 360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94) | Jan 25, 2024 |
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